{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Norwalk",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92857",
      "recalling_firm": "Ecometics, Inc.",
      "address_1": "19 Concord St",
      "address_2": "N/A",
      "postal_code": "06854-3706",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-1099-2023",
      "product_description": "Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.",
      "product_quantity": "a) 6,120 tubes, b) 540 tubes",
      "reason_for_recall": "CGMP Deviations: Products not manufactured under current good manufacturing practices.",
      "recall_initiation_date": "20230809",
      "center_classification_date": "20230824",
      "report_date": "20230830",
      "code_info": "a) and b) 1E113A, exp 4/24"
    }
  ]
}